Disease

Congenital Adrenal Hyperplasia 1

About the Disease
Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency, also known as 21-hydroxylase deficiency, is related to lipoid congenital adrenal hyperplasia and ehlers-danlos syndrome. An important gene associated with Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency is CYP21A2 (Cytochrome P450 Family 21 Subfamily A Member 2). The drugs Racepinephrine and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include adrenal cortex, testes and cortex, and related phenotypes are decreased circulating cortisol level and elevated circulating 17-hydroxyprogesterone

Common Targets
POR | CYP21A2 | NR3C1 | LINC02210-CRHR1 | CRHR1

疾病靶点研报
Congenital adrenal hyperplasia 1

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